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CY1123487T1 - Modulators of cystic fiber transmembrane conductance regulator - Google Patents

Modulators of cystic fiber transmembrane conductance regulator

Info

Publication number
CY1123487T1
CY1123487T1 CY20201101013T CY201101013T CY1123487T1 CY 1123487 T1 CY1123487 T1 CY 1123487T1 CY 20201101013 T CY20201101013 T CY 20201101013T CY 201101013 T CY201101013 T CY 201101013T CY 1123487 T1 CY1123487 T1 CY 1123487T1
Authority
CY
Cyprus
Prior art keywords
modulators
conductance regulator
transmembrane conductance
cystic fiber
cystic
Prior art date
Application number
CY20201101013T
Other languages
Greek (el)
Inventor
Mark Thomas Miller
Corey Anderson
Vijayalaksmi Arumugam
Brian Richard Bear
Hayley Marie Binch
Jeremy J. Clemens
Thomas Cleveland
Erica Conroy
Timothy Richard Coon
Bryan A. Frieman
Peter Diederik Jan Grootenhuis
Raymond Stanley GROSS
Sara Sabina Hadida-Ruah
Haripada Khatuya
Pramod Virupax Joshi
Paul John Krenitsky
Chun-Chieh Lin
Gulin Erdogan Marelius
Vito Melillo
Jason Mccartney
Original Assignee
Vertex Pharmaceuticals Incorporated
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=55631997&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CY1123487(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Vertex Pharmaceuticals Incorporated filed Critical Vertex Pharmaceuticals Incorporated
Publication of CY1123487T1 publication Critical patent/CY1123487T1/en

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    • AHUMAN NECESSITIES
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404Indoles, e.g. pindolol
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    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • A61K31/4525Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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Abstract

Η παρούσα εφεύρεση χαρακτηρίζει ένωση του τύπου Ι ή φαρμακευτικώς αποδεκτό άλας αυτής, όπου R1, R2, R3, W, X, Υ, Ζ, n, o, p, και q ορίζονται στο παρόν, για τη θεραπεία προκαλούμενων από CFTR ασθενειών, όπως κυστικής ίνωσης. Η παρούσα εφεύρεση επίσης χαρακτηρίζει φαρμακευτικές συνθέσεις, μέθοδο θεραπείας, και κιτ αυτών.The present invention features a compound of formula I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, W, X, Y, Z, n, o, p, and q are defined herein, for the treatment of CFTR-mediated diseases such as cystic fibrosis. The present invention also features pharmaceutical compositions, method of treatment, and kits thereof.

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